CNR Institutional Research Information System

D'ESPOSITO, MAURIZIO
 Distribuzione geografica
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Continente #
EU - Europa 34
AS - Asia 33
NA - Nord America 4
Totale 71
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Nazione #
IT - Italia 30
KR - Corea 13
SG - Singapore 13
CN - Cina 5
US - Stati Uniti d'America 4
DE - Germania 3
VN - Vietnam 2
NL - Olanda 1
Totale 71
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Città #
Naples 20
Seoul 13
Singapore 12
Aversa 10
Guangzhou 4
Hanover 3
Hanoi 2
Amsterdam 1
Forest City 1
Totale 66
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Nome #
Epigenetic control of hypoxia inducible factor-1?-dependent expression of placental growth factor in hypoxic conditions 12
Molecular dissection of two human chromatin diseases, Rett syndrome and ICF syndrome 7
Agonist stimulated 5-HT7R recovers gene expression profile in cortical neurons of a Rett syndrome mouse model 4
Molecular dissection of two human chromatin disease, Rett syndrome and ICF syndrome 4
Select item 10671Mutation in the nerve-specific 5'non-coding region of Cx32 gene and absence of specific mRNA in a CMTX1 Italian family. Mutations in brief no. 195. Online. 3
Gene Expression Profile in Liver Transplantation and the Influence of Gene Dysregulation Occurring in Deceased Donor Grafts 3
DNA methylation in X inactivation, imprinting and associated diseases 2
Genomic characterization and chromosomal mapping of 5 river buffalo skeletal muscle differentiation master genes 2
High resolution methylation analysis of HMLH1 promoter in sporadic endometrial and colorectal carcinomas. 2
Expression of HOX homeogenes in human neuroblastoma cell culture lines 2
Mutation in the nerve-specific 5'non-coding region of Cx32 gene and absence of specific mRNA in a CMTX1 Italian family. Mutations in brief no. 195. Online. 2
Glycosphingolipid metabolic reprogramming drives neural differentiation 2
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region 2
Expression of HOX homeogenes in human neuroblastoma cell culture lines. 1
Transcriptomic and epigenomic landscape in rett syndrome 1
Abnormal N-glycosylation pattern for brain nucleotide pyrophosphatase-5 (NPP-5) in Mecp2-mutant murine models of Rett syndrome. 1
Chapter 18. Non-invasive Prenatal Diagnosis: An epigenetic approach to the detection of common fetal chromosome disorders by analysis of maternal blood samples. 1
DIFFERENTIAL REGULATION BY RETINOIC ACID OF THE HOMEOBOX GENES OF THE 4 HOX LOCI IN HUMAN EMBRYONAL CARCINOMA-CELLS 1
Non-invasive Prenatal Diagnosis: An epigenetic approach to the detection of common fetal chromosome disorders by analysis of maternal blood samples 1
Incontinentia Pigmenti Type 2 (IP2): isolation and characterisation of the gene through trascriptional and sequence analysis 1
Epigenetic alteration of microRNAs in DNMT3B-mutated patients of ICF syndrome 1
Complex Events In The Evolution Of The Human Pseudoautosomal Region 2 (PAR2) 1
Differential expression of human HOX-2 gene along the anterior-posterior axis in embryonic central nervous system. 1
MECP2 Duplication Syndrome: Evidence of Enhanced Oxidative Stress. A Comparison with Rett Syndrome 1
CODING AND NON-CODING RNAS IN A LONG SHELF-LIFE TOMATO VARIETY 1
Physical mappaing of a retinal-specific trascription factor and the epigenetic mark H3K9me3 correlated to rhodopsin and genome wide retinal loci. 1
Non-coding RNAs in chromatin disease involving neurological defects 1
EPITOM: an integrated study of epigenomics in tomato fruit during post-harvest 1
DDX11L: a novel transcript family emerging from human subtelomeric regions 1
Oxidative brain damage in Mecp2-mutant murine models of Rett syndrome 1
DNA methylation 40 years later: its role in human health and disease 1
DNA methylation 40 years later: its role in human health and disease 1
Effects of Mecp2 loss of function in embryonic cortical neurons: a bioinformatics strategy to sort out non-neuronal cells variability from transcriptome profiling 1
MeCP2 and Major Satellite Forward RNA Cooperate for Pericentric Heterochromatin Organization 1
ATRX contributes to MECP2-mediated pericentric heterochromatin organization during neural differentiation 1
Absence of TI-VAMP/Vamp7 Leads to Increased Anxiety in Mice. 1
Molecular dissection of two human chromatin diseases, Rett syndrome and ICF syndrome 1
Totale 71
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Categoria #
all - tutte 1.673
article - articoli 1.219
book - libri 9
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 50
Totale 2.951
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202431 0 0 0 0 0 0 0 0 2 0 28 1
2024/202540 33 7 0 0 0 0 0 0 0 0 0 0
Totale 71